Reacción #66032

Ecuación de reacción

1-Bromo-4-methoxynaphthalene

4-(naphthalen-1-yl)phenylboronic acid

potassium carbonate

water

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product

Rendimiento 52.6%

1-methoxy-4-{4-(naphthalen-1-yl)phenyl}naphthalene

Rendimiento 52.6%

Disolventes

toluene

toluene

tetrahydrofuran

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturaunder reflux
2. 2
   OtroAfter completion of the reaction
3. 3
   Extracciónextracted with ethyl acetate (300 mL) and water (1000 mL)
4. 4
   SecadoThe organic layer was dried with magnesium sulfate
5. 5
   Concentraciónconcentrated under reduced pressure
6. 6
   Otroto obtain a solid
7. 7
   Filtraciónfiltered
8. 8
   OtroThe filtrate was recrystallized in methanol (800 mL)
9. 9
   FiltraciónThe resultant solid was filtered
10. 10
    Lavadowashed with hexane (300 mL)

Procedimiento

1-Bromo-4-methoxynaphthalene (25 g, 0.105 mol), 4-(naphthalen-1-yl)phenylboronic acid (30.4 g, 0.137 mol), potassium carbonate (21.9 g, 0.16 mol), tetrakis(triphenylphosphine)palladium(0) (2.4 g, 0.01 mol), water (25 mL), tetrahydrofuran (75 mL) and toluene (75 mL) were stirred in a 250 mL round-bottom flask for 12 hours under reflux. After completion of the reaction, the reaction mixture was cooled to room temperature and extracted with ethyl acetate (300 mL) and water (1000 mL). The organic layer was dried with magnesium sulfate and concentrated under reduced pressure to obtain a solid. The solid was dissolved in hot toluene (400 mL) and then filtered. The filtrate was recrystallized in methanol (800 mL). The resultant solid was filtered and washed with hexane (300 mL) to obtain a product (20 g, 0.055 mol, 52.6%).

Fuente